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Omega-3 fatty acid supplementation in adolescents with borderline personality disorder and ultra-high risk criteria for psychosis: a post hoc subgroup analysis of a double-blind, randomized controlled trial.
Can J Psychiatry. 2013 Jul; 58(7):402-8.CJ

Abstract

OBJECTIVE

To investigate whether long-chain omega-3 (n-3) polyunsaturated fatty acids (PUFAs) improve functioning and psychiatric symptoms in young people with borderline personality disorder (BPD) who also meet ultra-high risk criteria for psychosis.

METHODS

We conducted a post hoc subgroup analysis of a double-blind, randomized controlled trial. Fifteen adolescents with BPD (mean age 16.2 years, [SD 2.1]) were randomized to either 1.2 g/day n-3 PUFAs or placebo. The intervention period was 12 weeks. Study measures included the Positive and Negative Syndrome Scale, the Montgomery-Åsberg Depression Rating Scale, and the Global Assessment of Functioning. Side effects were documented with the Udvalg for Kliniske Undersøgelser. Fatty acids in erythrocytes were analyzed using capillary gas chromatography.

RESULTS

At baseline, erythrocyte n-3 PUFA levels correlated positively with psychosocial functioning and negatively with psychopathology. By the end of the intervention, n-3 PUFAs significantly improved functioning and reduced psychiatric symptoms, compared with placebo. Side effects did not differ between the treatment groups.

CONCLUSIONS

Long-chain n-3 PUFAs should be further explored as a viable treatment strategy with minimal associated risk in young people with BPD. (

CLINICAL TRIAL REGISTRATION NUMBER

NCT00396643).

Authors+Show Affiliations

Department of Child and Adolescent Psychiatry, Medical University of Vienna, Vienna, Austria. amminger@unimelb.edu.auNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

23870722

Citation

Amminger, G Paul, et al. "Omega-3 Fatty Acid Supplementation in Adolescents With Borderline Personality Disorder and Ultra-high Risk Criteria for Psychosis: a Post Hoc Subgroup Analysis of a Double-blind, Randomized Controlled Trial." Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie, vol. 58, no. 7, 2013, pp. 402-8.
Amminger GP, Chanen AM, Ohmann S, et al. Omega-3 fatty acid supplementation in adolescents with borderline personality disorder and ultra-high risk criteria for psychosis: a post hoc subgroup analysis of a double-blind, randomized controlled trial. Can J Psychiatry. 2013;58(7):402-8.
Amminger, G. P., Chanen, A. M., Ohmann, S., Klier, C. M., Mossaheb, N., Bechdolf, A., Nelson, B., Thompson, A., McGorry, P. D., Yung, A. R., & Schäfer, M. R. (2013). Omega-3 fatty acid supplementation in adolescents with borderline personality disorder and ultra-high risk criteria for psychosis: a post hoc subgroup analysis of a double-blind, randomized controlled trial. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie, 58(7), 402-8.
Amminger GP, et al. Omega-3 Fatty Acid Supplementation in Adolescents With Borderline Personality Disorder and Ultra-high Risk Criteria for Psychosis: a Post Hoc Subgroup Analysis of a Double-blind, Randomized Controlled Trial. Can J Psychiatry. 2013;58(7):402-8. PubMed PMID: 23870722.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Omega-3 fatty acid supplementation in adolescents with borderline personality disorder and ultra-high risk criteria for psychosis: a post hoc subgroup analysis of a double-blind, randomized controlled trial. AU - Amminger,G Paul, AU - Chanen,Andrew M, AU - Ohmann,Susanne, AU - Klier,Claudia M, AU - Mossaheb,Nilufar, AU - Bechdolf,Andreas, AU - Nelson,Barnaby, AU - Thompson,Andrew, AU - McGorry,Patrick D, AU - Yung,Alison R, AU - Schäfer,Miriam R, PY - 2013/7/23/entrez PY - 2013/7/23/pubmed PY - 2013/8/28/medline KW - adolescents KW - borderline personality disorder KW - omega-3 fatty acids KW - randomized controlled trial KW - ultra-high risk SP - 402 EP - 8 JF - Canadian journal of psychiatry. Revue canadienne de psychiatrie JO - Can J Psychiatry VL - 58 IS - 7 N2 - OBJECTIVE: To investigate whether long-chain omega-3 (n-3) polyunsaturated fatty acids (PUFAs) improve functioning and psychiatric symptoms in young people with borderline personality disorder (BPD) who also meet ultra-high risk criteria for psychosis. METHODS: We conducted a post hoc subgroup analysis of a double-blind, randomized controlled trial. Fifteen adolescents with BPD (mean age 16.2 years, [SD 2.1]) were randomized to either 1.2 g/day n-3 PUFAs or placebo. The intervention period was 12 weeks. Study measures included the Positive and Negative Syndrome Scale, the Montgomery-Åsberg Depression Rating Scale, and the Global Assessment of Functioning. Side effects were documented with the Udvalg for Kliniske Undersøgelser. Fatty acids in erythrocytes were analyzed using capillary gas chromatography. RESULTS: At baseline, erythrocyte n-3 PUFA levels correlated positively with psychosocial functioning and negatively with psychopathology. By the end of the intervention, n-3 PUFAs significantly improved functioning and reduced psychiatric symptoms, compared with placebo. Side effects did not differ between the treatment groups. CONCLUSIONS: Long-chain n-3 PUFAs should be further explored as a viable treatment strategy with minimal associated risk in young people with BPD. ( CLINICAL TRIAL REGISTRATION NUMBER: NCT00396643). SN - 0706-7437 UR - https://www.unboundmedicine.com/medline/citation/23870722/Omega_3_fatty_acid_supplementation_in_adolescents_with_borderline_personality_disorder_and_ultra_high_risk_criteria_for_psychosis:_a_post_hoc_subgroup_analysis_of_a_double_blind_randomized_controlled_trial_ L2 - https://journals.sagepub.com/doi/10.1177/070674371305800705?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed DB - PRIME DP - Unbound Medicine ER -